Cargando…

Evaluation of the teaching recovery techniques community-based intervention for accompanied refugee children experiencing post-traumatic stress symptoms (Accompanied refugeeS In Sweden Trial; ASsIST): study protocol for a cluster randomised controlled trial

BACKGROUND: Refugee children have often experienced traumas and are at significant risk of developing mental health problems, such as symptoms of post-traumatic stress disorder (PTSD), depression and anxiety, which can continue for years after resettlement. The Accompanied refugeeS In Sweden Trial (...

Descripción completa

Detalles Bibliográficos
Autores principales: Warner, Georgina, Durbeej, Natalie, Salari, Raziye, Fängström, Karin, Lampa, Elin, Baghdasaryan, Zaruhi, Osman, Fatumo, Gupta Löfving, Sandra, Perez Aronsson, Anna, Feldman, Inna, Sampaio, Filipa, Ssegonja, Richard, Bjärtå, Anna, Rondung, Elisabet, Leiler, Anna, Wasteson, Elisabet, Calam, Rachel, Oppedal, Brit, Keeshin, Brooks, Sarkadi, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383950/
https://www.ncbi.nlm.nih.gov/pubmed/32713847
http://dx.doi.org/10.1136/bmjopen-2019-035459
Descripción
Sumario:BACKGROUND: Refugee children have often experienced traumas and are at significant risk of developing mental health problems, such as symptoms of post-traumatic stress disorder (PTSD), depression and anxiety, which can continue for years after resettlement. The Accompanied refugeeS In Sweden Trial (ASsIST) aims to evaluate a community-based intervention, called ‘Teaching Recovery Techniques’ (TRT), for accompanied refugee minors experiencing PTSD symptoms. METHODS/DESIGN: A cluster randomised controlled trial will be conducted in which participants will be randomly allocated to one of the two possible arms: the intervention arm (n=113) will be offered the TRT programme and the waitlist-control arm (n=113) will receive services as usual, followed by the TRT programme around 20 weeks later. Outcome data will be collected at three points: pre-intervention (T1), post-intervention (T2; c.8 weeks after randomisation) and follow-up (T3; c.20 weeks after randomisation). ETHICS AND DISSEMINATION: Ethical approval was granted by the Regional Ethical Review Board in Uppsala (Ref. 2018/382) (24(th) February 2019). Results will be published in scientific journals. TRIAL REGISTRATION DETAILS: ISRCTN17754931. Prospectively registered on 4(th) June 2019.